Readmission and Dehydration Prevention in Patients With Elective Ileostomy
Condition(s) studied
Study summary
The goal of this prospective observational study is to evaluate the adherence to DRIP score calculation and the application rate of each proposed item to prevent dehydration and readmission in patients undergoing ileostomy creation after elective colorectal resection different Italian colorectal surgical centers.
The primary endpoint is to verifythe application rate of DRIP score calculation and protocol items.
Secondary endpoints are 30, 90, and 180-day total and dehydration readmission rates.
Eligibility
Primary outcome measure(s)
- DRIP score calculation and protocol items — From enrollment to the end of recruitment at 6 months
Application rate of DRIP score calculation and protocol items
Trial sites (7)
| Facility | City | Region | Status |
|---|---|---|---|
| ASST Ovest Milanese, Ospedale di Legnano | Legnano | Italy | Recruiting |
| Luigi Sacco University Hospital | Milan | Italy | Recruiting |
| Università degli Studi Milano-Bicocca, Ospedale San Gerardo | Monza | Italy | Recruiting |
| University of Palermo, "Paolo Giaccone" University Hospital | Palermo | Italy | Recruiting |
| Ospedale Santa Maria della Misericordia | Rovigo | Italy | Recruiting |
| ASST Nord Milano, Ospedale Città di Sesto San Giovanni | Sesto San Giovanni | Italy | Recruiting |
| IRCCS Policlinico di Bologna | Bologna | Italy | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06824623 on ClinicalTrials.gov ↗ ← All trials in Italy